Abstract
Hepatitis C virus non-structural NS5A protein inhibits epidermal growth factor (EGF)-stimulated activation of the Ras-ERK mitogen-activated protein kinase pathway at a point upstream of Ras activation. To determine the mechanism of this inhibition, the events occurring between the EGF receptor and Ras in Huh-7 cells harbouring the HCV subgenomic replicon were investigated. It was shown that, following EGF stimulation, these cells exhibited decreased EGF receptor tyrosine phosphorylation, aberrant recruitment of the adaptor proteins ShcA and Grb2 to the EGF receptor, reduced phosphorylation of ShcA and reduced Ras activation in comparison with control cells. These data are consistent with effects of NS5A and/or other components of the replicon on multiple events occurring upstream of Ras.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adaptor Proteins, Signal Transducing / metabolism
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Cell Line, Tumor
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ErbB Receptors / metabolism*
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Extracellular Signal-Regulated MAP Kinases / metabolism
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GRB2 Adaptor Protein
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Gene Expression Regulation
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Genome, Viral*
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Hepacivirus / genetics
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Hepacivirus / metabolism
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Hepacivirus / pathogenicity*
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Humans
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Replicon / physiology*
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Shc Signaling Adaptor Proteins
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Signal Transduction / drug effects
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Src Homology 2 Domain-Containing, Transforming Protein 1
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ras Proteins / metabolism*
Substances
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Adaptor Proteins, Signal Transducing
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GRB2 Adaptor Protein
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GRB2 protein, human
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SHC1 protein, human
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Shc Signaling Adaptor Proteins
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Src Homology 2 Domain-Containing, Transforming Protein 1
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ErbB Receptors
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Extracellular Signal-Regulated MAP Kinases
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ras Proteins